miR-21,减轻创伤性脑损伤后血脑屏障损伤的潜在治疗靶点

X. Ge, P. Lei, Jian-ning Zhang
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引用次数: 2

摘要

外伤性脑损伤(TBI)是一种发病率高、致残率高、死亡率高的疾病。血脑屏障(BBB)损伤是脑外伤后重要的脑病理改变,影响疾病的发展和预后。在我们之前的研究中,我们报道了神经元中miR-21-5p可以发挥抗凋亡作用,促进脑外伤后损伤血脑屏障的修复。上调脑内miR-21-5p水平可增强miR-21-5p的上述功能,从而减轻血脑屏障损伤,改善脑外伤预后。miR-21-3p是由pre-miR-21与miR-21-5p同时产生的,据报道,miR-21-3p在调节血管生成因子的表达中发挥重要作用,而血管生成因子可以影响下游的免疫炎症反应和细胞凋亡。我们总结了以往关于miR-21-3p的报道,推断miR-21-3p可能影响脑外伤后血脑屏障损伤的发展。综上所述,miR-21是影响创伤性血脑屏障损伤恢复的重要miRNA,因此它可能是TBI干预的潜在治疗靶点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
miR-21, a potential therapeutic target of alleviating blood-brain barrier damage after traumatic brain injury
Traumatic brain injury (TBI) is a disease with high morbidity and leads to high rate of disability and mortality. The blood-brain barrier (BBB) damage is an important pathological change in brain after TBI, which impacts the development and prognosis of the disease. In our previous research, we have reported that miR-21-5p in neurons can exert an anti-apoptosis effect, and promote the restoration of injured BBB after TBI. Up-regulation of miR-21-5p level in brain can amplify the above functions of miR-21-5p, thus alleviate BBB damage and improve the prognosis of TBI. miR-21-3p, which is generated from pre-miR-21 at the same time with miR-21-5p, has been reported to play significant roles in regulating the expression of angiogenic factors, which can impact downstream immuno-inflammatory responses and cellular apoptosis. We made a summary of previous reports on miR-21-3p and inferred that miR-21-3p could influence the development of BBB damage after TBI. Taken together, miR-21 is a vital miRNA that impacts the restoration of traumatic BBB damage, thus it could be a potential therapeutic target for interventions in TBI.
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